利桑珠单抗对滑膜炎、痤疮、脓疱病、骨质增生和骨膜炎(SAPHO)缓解的疗效:关于风湿病和皮肤病表现的病例报告及文献综述。

IF 0.7 Q4 IMMUNOLOGY
Case Reports in Immunology Pub Date : 2024-03-19 eCollection Date: 2024-01-01 DOI:10.1155/2024/9076852
Mario Ferraioli, Luigi Fiannacca, Elisabetta Greco, Eneida Cela, Mauro Fatica, Alberto Bergamini, Maria Sole Chimenti
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引用次数: 0

摘要

SAPHO 综合征是一种复杂的疾病,既包括炎症性关节炎和/或骨炎,也包括皮肤表现。它被认为是一种罕见的疾病,事实上,还没有对其治疗和管理进行过临床试验。因此,治疗方法主要基于小型病例研究。在此,我们描述了一名 63 岁女性 SAPHO 综合征患者的病例,她在使用甲氨蝶呤、英夫利昔单抗、阿达木单抗治疗失败后,使用选择性 IL-23p19 拮抗剂利桑珠单抗进行治疗,并对赛库木单抗产生了过敏反应。在2022年11月开始治疗时,患者出现双膝关节炎,伴有掌脓疱病和躯干上的凹陷性银屑病。DAPSA 评分为 24 分,PtGA 为 80 毫米,PASI 评分为 11.1 分,BSA 为 40%。此后,利桑珠单抗以 150 毫克的标准剂量开始使用。第 24 周时,患者达到临床缓解,DAPSA 评分为 8 分,PtGA 为 30 毫米,PASI 为 1 分,BSA 为 2.5 分。在随后的第 52 周评估中,患者保持了临床缓解状态。同时,患者未报告任何不良反应。与健康相关的生活质量也在上述相同的时间点进行了评估,结果显示有显著改善。总之,本病例报告希望指出利桑珠单抗对 SAPHO 综合征的疗效和安全性,报告称患者在长达 12 个月的随访期间病情得到了持续缓解。我们可以将IL-23p19靶向疗法视为SAPHO的一种新型治疗方案--具有很高的疗效潜力,尤其是对于已经接受过其他生物制剂治疗的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risankizumab Efficacy in Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO) Remission: A Case Report on Rheumatologic and Dermatologic Disease Manifestations with Literature Review.

SAPHO syndrome is a complex disease that encompasses both inflammatory arthritis and/or osteitis and dermatologic manifestations. It is considered a rare disease, in fact, no clinical trials have been conducted on its therapy and management. Therefore, therapeutic approach is based on small case studies. Here, we described the case of a 63-year-old woman affected by SAPHO syndrome, treated with the selective IL-23p19 antagonist, Risankizumab, after unsuccessful therapies with Methotrexate, Infliximab, Adalimumab, and an allergic reaction to Secukinumab. At the beginning of therapy, in November 2022, the patient presented with arthritis in both knees associated with palmar pustulosis and guttate psoriasis on the trunk. DAPSA score was 24, PtGA 80 mm, PASI score 11.1, and BSA 40%. Thereafter, Risankizumab was started at the standard dosage of 150 mg. At week 24 patient achieved clinical remission, DAPSA score was 8, PtGA was 30 mm, PASI was 1, and BSA 2.5. Patient maintained clinical remission state at the subsequent week 52 evaluation. At the same time, the patient did not report any adverse effects. Health-related quality of life was also assessed at the same time points aforementioned, showing significant improvement. In conclusion, this case report wants to point out the efficacy and safety of Risankizumab in SAPHO syndrome, reporting a sustained disease remission through a 12 months long follow-up period. We can consider IL-23p19 targeted therapy as a novel treatment option for SAPHO-with a high efficacy potential-especially on patients that have already been treated with other biologics.

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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
14
审稿时长
15 weeks
期刊介绍: Case Reports in Immunology is a peer-reviewed, Open Access journal that publishes case reports and case series related to allergies, immunodeficiencies, autoimmune diseases, immune disorders, cancer immunology and transplantation immunology.
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